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DBL Bortezomib bortezomib 1.0 mg powder for injection vial - TGA Drug Approval Details
Approvals
/
TGA
/
DBL Bortezomib bortezomib 1.0 mg powder for injection vial
Approved
STANDARD
DBL Bortezomib bortezomib 1.0 mg powder for injection vial
Pfizer Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
c8d8c0d8d7285a50
Company
Pfizer Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
c8d8c0d8d7285a50
Product Name
DBL Bortezomib bortezomib 1.0 mg powder for injection vial
Artg Id
313359
Artg Name
DBL Bortezomib bortezomib 1.0 mg powder for injection vial
Sponsor
Pfizer Australia Pty Ltd
Company Detail Path
/organization/pfizer-australia-pty-ltd
Artg Date
2020-02-10
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/fe875102a8261a47370231d511f3e10b.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/8e2954d456fbe3e35ad4acde905ef547.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
c8d8c0d8d7285a50
Type
Standard
Back to TGA Approvals